recall
Alert: Akorn PrednisoLONE oral solution (15 mg/5mL, 240 mL bottles)
Akorn recalls one lot of PrednisoLONE oral solution (15 mg/5mL, 240 mL bottles) due to defective containers.
recall
Alert: All ranitidine products (Zantac)
FDA requests removal of all ranitidine products (Zantac) from the market due to contamination with N-Nitrosodimethylamine (NDMA).
recall
Alert: Altaire Pharmaceuticals, Inc. recalls Perrigo brand ophthalmic products
Concerns about quality assurance controls
recall
Alert: American Health Packaging Valsartan Tablets, USP, 160 mg
Presence of probable human carcinogen N-Nitrosodiethylamine
recall
Alert: Amlodipine and Valsartan Tablets, USP; Valsartan Tablets, USP; and Valsartan and Hydrochlorothiazide Tablets, USP
Presence of probable carcinogen N-nitrosodiethylamine
recall
Alert: Amlodipine/Valsartan Combination Tablets and Amlodipine/Valsartan/Hydrochlorothiazide Combination Tablets
Presence above specification limits of probable carcinogen N-nitroso-diethylamine
recall
Alert: Amlodipine Valsartan Tablets USP, Valsartan HCTZ Tablets, USP and Valsartan Tablets USP
Presence of probable human carcinogen N-nitrosodiethylamine
recall
Alert: Arrow MAC Two-Lumen Central Venous Access Kits
Teleflex and their subsidiary Arrow International, LLC recall Arrow MAC Two-Lumen Central Venous Access Kits and Arrow Pressure Injectable Arrowg+ard…
recall
Alert: Aurobindo Pharma/ScieGen Pharmaceuticals Irbesartan
Presence of probable carcinogen N-nitrosodiethylamine
recall
Alert: Aurobindo Pharma mirtazapine tablets
Aurobindo Pharma USA, Inc. recalls mirtazapine tablets due to a label error on declared strength.
recall
Alert: Aurobindo Quinapril and Hydrochlorothiazide Tablets USP 20mg/12.5mg
Aurobindo Pharma USA, Inc. recalls two lots of Quinapril and Hydrochlorothiazide Tablets USP 20mg / 12.5mg, due to presence of Nitrosamine Drug…
recall
Alert: AurobindoPharma Amlodipine Valsartan Tablets USP and Valsartan Tablets, USP (Expanded Recall)
Due to presence of probable carcinogen N-nitrosodiethylamine
recall
Alert: AurobindoPharma Acetris Valsartan Tablets, USP
Due to presence of probable carcinogen N-nitrosodiethylamine
recall
Alert: AuroMedics Acyclovir Sodium Injection 500 mg per 10 mL (50 mg/mL), 10 mL single dose vial
Eugia US LLC recalls lot number AC22006 of AuroMedics Acyclovir Sodium Injection 500 mg per 10 mL (50 mg/mL), 10 mL single dose vial due to a…
recall
Alert: IV bags containing fentanyl or oxytocin & various prefilled syringes
Nephron Sterile Compounding Center recalls 2.1 million doses of medicine and medical equipment due to a lack of assurance of sterility.
recall
Alert: Baxter Clearlink Basic Solution Set with Duovent
Baxter Healthcare recalls over half a million Clearlink Basic Solution Sets with Duovent (used for chemotherapy) due to a risk of leaks that may…
recall
Alert: Baxter DiscPac Syringe Tip Caps
Baxter recalls certain packages of DiscPac Syringe Tip Caps, Self-Righting, Luer Slip, because of the potential for the packaging to fail to maintain…
recall
Alert: B. Braun Medical Inc. blood administration sets
B. Braun Medical Inc. blood administration sets recalled due to potential leakage at joint between blood filter and tubing.
recall
Alert: Bryant Ranch morphine sulfate extended-release tablets
Bryant Ranch has recalled one lot each of 30-mg and 60-mg morphine sulfate extended-release tablets due to incorrect dosage labeling.
recall
Alert: Camber Pharmaceuticals Losartan Potassium Tablets, USP, 25 mg, 50 mg and 100 mg
Presence of potential carcinogen N-Nitroso N-Methyl 4-amino butyric acid
recall
Alert: BD CareFusion 303, Inc. Alaris Pump Module Model 8100 Bezel Assembly
The bezel posts may become cracked and separated which could lead to inaccurate delivery of fluids to the patient.
recall
Alert: GE CARESCAPE Respiratory Modules and Airway Gas Option
GE CARESCAPE Respiratory Modules and Airway Gas Option recalled due to a manufacturing issue.
recall
Alert: GE Carestation 600 Series anesthesia systems
GE Carestation 600 Series anesthesia systems recalled due to loss of mechanical ventilation.
recall
Alert: Ceftriaxone for Injection USP, 250mg, 500mg, 1g and 2g
Presence of visual grey particulate matter in reconstituted vials
